Who we are: Soname Solutions is a group of enthusiasts who are in love with data analytics and big data. We help our clients in becoming data-driven companies. Our team keeps expanding, and it includes 60+ professionals from Germany, Poland and Georgia. We blend deep expert knowledge with humanity. We have been working in data analysis for the last 15 years. This vast experience, analytical skills of our team members, hunger for knowledge define our way of working with each other and our clients. This is all seasoned with kindness, curiosity, empathy, willingness to help, trust, and transparency. The best qualities of our team serve us in finding optimal technical solutions that please our customers. All of that is a base for long-term relations with international corporations. They are always wowed with our services. Position: We are looking for a Senior Data Warehouse Developer to become a part of our team. About the project: As part of this project, we cooperate with German telecom company. Tech stack: SQL, DWH, Power BI, Oracle, PostgreSQL.

Role Description We are looking for a Senior Data Warehouse Developer to become a part of our team. As a Data Engineer, you will be responsible for: - Familiarization with complex business processes and their technical implementation in the DWH - Designing and implementing ETL/ELT processes in a comprehensive, multi-layered DWH - Performance optimization at the database and ETL level - Creating architecture proposals for new developments within our DWH - Close collaboration with business departments to align requirements and find joint solutions - Independent work with a high degree of personal responsibility Qualifications - Deep expertise in classic 3-layer DWH architectures (Staging/Core/Data Marts) - Strong knowledge of 3NF modeling, Inmon architectures, and dimensional modeling (Kimball) - Experience with technical data versioning (historization) - Solid experience in performance optimization, including: - Analyzing and improving execution plans - Implementing and managing partitioning concepts - Monitoring and controlling large data volumes - Excellent knowledge of SQL; PL/SQL is a distinct advantage - Proficiency in German (very good level) and strong communication skills Requirements - Independent and structured way of working - Ability to explain complex technical solutions clearly and understandably - Proactive involvement in shaping the future DWH architecture Benefits - Long-term projects (12m+) with leading global companies with a worldwide reputation - Strong relationships with clients - Friendly, well-coordinated, and helpful team - Mentoring in the first months of work - Paid sick leave and 5 days off a year - Up to 26-days of paid vacation - Medical care payment - Competitive salary, regular performance, and salary review process - Fully remote position - Interesting corporate events - Gifts and pleasant surprises for significant events - Daily English / German communication

Role Description Precision for Medicine is hiring a Clinical Data Associate II to join our team. Candidates can be based in Hungary, Poland, Romania, Serbia or Slovakia. The Clinical Data Associate II provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigned projects under direct supervision. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study specific plans and guidelines will be followed. This position may perform database development and testing, as well as additional data management activities. - Support the Lead DM as a back-up and/or team member, ensuring continuity, responsiveness, and that tasks are performed in a timely manner - May perform data entry for paper-CRF studies, as needed - May perform quality control of data entry - May develop CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders - May assist in building clinical databases - Conduct database build UAT and maintain quality controlled database build documentation - Assist in specifying requirements for all edit check types e.g. electronic, manual data review, edit checks, etc. - Responsible for creating, revising, appropriate versioning and maintaining data management documentation. - Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed - Review and query clinical trial data according to the Data Management Plan - Assist in line listing data review based on the guidance provided by the sponsor and/or Lead DM - Run patient and study level status and metric reporting - Perform medical coding of medical terms relative to each other in order to ensure medical logic and consistency - Assist with coordinating SAE/AE reconciliation - Assist with liaising with third-party vendors such as external data and EDC vendors in a project-manager capacity in support of timelines and data-related deliverables - May assist with SAS programming and quality control of SAS programs used in the Data Management department - May assist in identifying and troubleshooting operational problems, issues, obstacles, and barriers for studies based on metrics data, audit reports, and input from project team members and other stakeholders - May assist in reviewing and providing feedback on protocols, Statistical Analysis Plans (SAP) and Clinical Study Reports (CSRs), if required by the project - May assist in participating in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to data management and database management activities - Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues - May present software demonstrations/trainings, department/company training sessions, present at project meetings - May require some travel - Perform other duties as assigned Qualifications - Bachelors and/or a combination of related experience - Around 2 years’ experience working as a Clinical Data Associate for a CRO/Pharma/Biotech company. - Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook - Able to handle a variety of clinical research tasks - Excellent organizational and communication skills - Professional use of the English language; both written and oral Company Description Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. We apply our expertise to trials at all stages—from early development through approval—with embedded experience in oncology and rare disease.

Role Description Precision for Medicine is hiring a Clinical Data Associate II to join our team. Candidates can be based in Hungary, Poland, Romania, Serbia or Slovakia. The Clinical Data Associate II provides data management support and assistance in all aspects of the clinical trial data management process from study start up to post database lock for assigned projects under direct supervision. Standard Operating Procedures / Work Instructions (SOPs/WIs); regulatory directives; study specific plans and guidelines will be followed. This position may perform database development and testing, as well as additional data management activities. - Support the Lead DM as a back-up and/or team member, ensuring continuity, responsiveness, and that tasks are performed in a timely manner - May perform data entry for paper-CRF studies, as needed - May perform quality control of data entry - May develop CRF specifications from the clinical study protocol and coordinate the review/feedback from all stakeholders - May assist in building clinical databases - Conduct database build UAT and maintain quality controlled database build documentation - Assist in specifying requirements for all edit check types e.g. electronic, manual data review, edit checks, etc. - Responsible for creating, revising, appropriate versioning and maintaining data management documentation. - Train clinical research personnel on the study specific CRF, EDC, and other project related items as needed - Review and query clinical trial data according to the Data Management Plan - Assist in line listing data review based on the guidance provided by the sponsor and/or Lead DM - Run patient and study level status and metric reporting - Perform medical coding of medical terms relative to each other in order to ensure medical logic and consistency - Assist with coordinating SAE/AE reconciliation - Assist with liaising with third-party vendors such as external data and EDC vendors in a project-manager capacity in support of timelines and data-related deliverables - May assist with SAS programming and quality control of SAS programs used in the Data Management department - May assist in identifying and troubleshooting operational problems, issues, obstacles, and barriers for studies based on metrics data, audit reports, and input from project team members and other stakeholders - May assist in reviewing and providing feedback on protocols, Statistical Analysis Plans (SAP) and Clinical Study Reports (CSRs), if required by the project - May assist in participating in the development and maintenance of Standard Operating Procedures (SOPs) and corresponding process documentation related to data management and database management activities - Communicate with study sponsors, vendors and project teams as needed regarding data, database or other relevant project issues - May present software demonstrations/trainings, department/company training sessions, present at project meetings - May require some travel - Perform other duties as assigned Qualifications - Bachelors and/or a combination of related experience - Around 2 years’ experience working as a Clinical Data Associate for a CRO/Pharma/Biotech company - Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook - Able to handle a variety of clinical research tasks - Excellent organizational and communication skills - Professional use of the English language; both written and oral Company Description Precision for Medicine is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. We apply our expertise to trials at all stages—from early development through approval—with embedded experience in oncology and rare disease.